A Study of Tocilizumab in Patients With Rheumatoid Arthritis
Completed
Conditions studied: Rheumatoid Arthritis
In brief
This is an open-label, uncontrolled, observational study in patients with rheumatoid arthritis (RA) who are receiving tocilizumab concomitantly with methotrexate as part of their standard of care.
Key facts
- Study ID
- NCT01187563
- Run by
- Regeneron Pharmaceuticals
- People needed
- 16
- Starts
- 2010-08-01
- Expected to finish
- 2010-12-01
- Last updated by the study team
- 2011-10-13
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- ≥ 18 years of age
- Moderately to severely active rheumatoid arthritis
- Inadequate response to previous treatment with an anti-TNF agent
- Receiving methotrexate for at least 12 wks before study
You may not qualify if…
- Previous treatment with tocilizumab
- Previous treatment with other IL-6 receptor inhibitors
- Treatment with corticosteroids (oral prednisone >10 mg/day or equivalent) within 4 wks
- Conditions noted in the tocilizumab prescribing information
Where it is running
- Study site — Worcester, Massachusetts, United States
- Study site — Duncansville, Pennsylvania, United States
Full record on ClinicalTrials.gov
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